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Anhui Annuy Latex Products Co., Ltd.

US

Last updated May 30, 2026

What Anhui Annuy Latex Products Co., Ltd. makes

The company manufactures non-powdered, non-antimicrobial examination and treatment gloves made from hevea latex and nitrile. These include patient examination gloves designed for medical procedures requiring barrier protection.

The portfolio consists of Class I medical devices listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Anhui Annuy Latex Products Co., Ltd. manufacture?

Anhui Annuy Latex Products Co., Ltd. specializes in non-powdered, non-antimicrobial examination and treatment gloves. Their portfolio includes gloves made from hevea latex and nitrile, specifically designed for patient examinations and medical procedures requiring barrier protection. These gloves are intended to reduce the risk of contamination during clinical interactions.

Where is Anhui Annuy Latex Products Co., Ltd. based?

The company is based in the United States. While the name suggests an origin in China (Anhui province), their manufacturing operations or regulatory filings are associated with the US market.

Which regulatory registries list Anhui Annuy Latex Products Co., Ltd.’s devices?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry tracks Class I medical devices that have been assigned a UDI, ensuring traceability and compliance with US regulatory requirements.

How are Anhui Annuy Latex Products Co., Ltd.’s gloves classified under medical device regulations?

The company’s gloves fall under Class I medical device classification. This classification applies to low-risk devices like examination gloves, where the risk to patients is minimal and regulatory oversight is relatively straightforward. Class I devices typically require listing with the FDA rather than premarket approval.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
421347466

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